FDAClass IIMay 29, 2019

Drill, cannulated, 4x150mm, AO recall

Drill, cannulated, 4x150mm, AO, Item Number ST502015403

Why was Drill, cannulated, 4x150mm, AO recalled?

An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All items marked with "Normed" are affected

Product
Drill, cannulated, 4x150mm, AO, Item Number ST502015403
Recalling firm
Zimmer GmbH
Quantity
N/A
Distribution
The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY.
Recall date
May 29, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls